FDA Device recall Z-1125-2022
KWIK-STIK" plus: Clostridium perfringens
- FDA Device
- Class III
- terminated
- Published 2022-06-01
On 2022-06-01 the FDA classified a Class III recall of KWIK-STIK" plus: Clostridium perfringens by Microbiologics, citing labeling error.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1125-2022 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2022-05-06 |
| Published | 2022-06-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Microbiologics |
| Distribution | US |
Product
KWIK-STIK" plus: Clostridium perfringens
Reason
Labeling error.
Identifiers
| code_info | catalog number: 0801P; lot number: 801-44-4; expiration date: 05/31/2023; UDI: 20845357019374 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1125-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.